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For: Andrade AC, Jee YH, Nilsson O. New Genetic Diagnoses of Short Stature Provide Insights into Local Regulation of Childhood Growth
. Horm Res Paediatr 2017;88:22-37. [PMID: 28334714 DOI: 10.1159/000455850] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 2.4] [Reference Citation Analysis]
Number Citing Articles
1 Mittal M, Gupta P, Kalra S, Bantwal G, Garg MK. Short Stature: Understanding the Stature of Ethnicity in Height Determination. Indian J Endocrinol Metab 2021;25:381-8. [PMID: 35300450 DOI: 10.4103/ijem.ijem_197_21] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
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3 Bogarín R, Richmond E, Rogol AD. A new approach to the diagnosis of short stature. Minerva Pediatr 2020;72:250-62. [PMID: 33045802 DOI: 10.23736/S0026-4946.20.05835-1] [Reference Citation Analysis]
4 Martin LJ, Benson DW. Identifying Genetic Modifiers in the Age of Exome: Current Considerations. J Pediatr 2019;213:8-10. [PMID: 31303336 DOI: 10.1016/j.jpeds.2019.06.041] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
5 Tao L, Wang C, Peng Y, Xu M, Wan M, Lou J, Yu X. Correlation Between Increase of Axial Length and Height Growth in Chinese School-Age Children. Front Public Health 2022;9:817882. [DOI: 10.3389/fpubh.2021.817882] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Wit JM, Deeb A, Bin-Abbas B, Al Mutair A, Koledova E, Savage MO. Achieving Optimal Short- and Long-term Responses to Paediatric Growth Hormone Therapy. J Clin Res Pediatr Endocrinol 2019;11:329-40. [PMID: 31284701 DOI: 10.4274/jcrpe.galenos.2019.2019.0088] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
7 Fan X, Zhao S, Yu C, Wu D, Yan Z, Fan L, Song Y, Wang Y, Li C, Ming Y, Gui B, Niu Y, Li X, Yang X, Luo S, Zhang Q, Zhao X, Pan H, Li M, Xia W, Qiu G, Liu P, Zhang S, Zhang J, Wu Z, Lupski JR, Posey JE, Chen S, Gong C, Wu N; Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study. Exome sequencing reveals genetic architecture in patients with isolated or syndromic short stature. J Genet Genomics 2021;48:396-402. [PMID: 34006472 DOI: 10.1016/j.jgg.2021.02.008] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Kang MJ. Novel genetic cause of idiopathic short stature. Ann Pediatr Endocrinol Metab 2017;22:153-7. [PMID: 29025200 DOI: 10.6065/apem.2017.22.3.153] [Cited by in Crossref: 15] [Cited by in F6Publishing: 16] [Article Influence: 3.0] [Reference Citation Analysis]
9 Zoccolillo M, Moia C, Comincini S, Cittaro D, Lazarevic D, Pisani KA, Wit JM, Bozzola M. Identification of novel genetic variants associated with short stature in a Baka Pygmies population. Hum Genet 2020;139:1471-83. [PMID: 32583022 DOI: 10.1007/s00439-020-02191-x] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
10 Crippa M, Giangiobbe S, Villa R, Bestetti I, De Filippis T, Fatti L, Taurino J, Larizza L, Persani L, Bellini F, Finelli P, Bonati MT. A balanced reciprocal translocation t (10;15) (q22.3; q26.1) interrupting ACAN gene in a family with proportionate short stature. J Endocrinol Invest. 2018;41:929-936. [PMID: 29302920 DOI: 10.1007/s40618-017-0819-3] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 2.3] [Reference Citation Analysis]
11 Amano N, Kitoh H, Narumi S, Nishimura G, Hasegawa T. A novel NPR2 mutation (p.Arg388Gln) in a patient with acromesomelic dysplasia, type Maroteaux. Clin Pediatr Endocrinol 2020;29:99-103. [PMID: 32694885 DOI: 10.1297/cpe.29.99] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
12 Domené S, Scaglia PA, Gutiérrez ML, Domené HM. Applying Bioinformatic Platforms, In Vitro, and In Vivo Functional Assays in the Characterization of Genetic Variants in the GH/IGF Pathway Affecting Growth and Development. Cells 2021;10:2063. [PMID: 34440832 DOI: 10.3390/cells10082063] [Reference Citation Analysis]
13 Cousminer DL, Wagley Y, Pippin JA, Elhakeem A, Way GP, Pahl MC, McCormack SE, Chesi A, Mitchell JA, Kindler JM, Baird D, Hartley A, Howe L, Kalkwarf HJ, Lappe JM, Lu S, Leonard ME, Johnson ME, Hakonarson H, Gilsanz V, Shepherd JA, Oberfield SE, Greene CS, Kelly A, Lawlor DA, Voight BF, Wells AD, Zemel BS, Hankenson KD, Grant SFA. Genome-wide association study implicates novel loci and reveals candidate effector genes for longitudinal pediatric bone accrual. Genome Biol 2021;22:1. [PMID: 33397451 DOI: 10.1186/s13059-020-02207-9] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
14 Tornese G. Letter to the Editor: "Genetic Testing for the Child With Short Stature - Has the Time Come to Change our Diagnostic Paradigm?". J Clin Endocrinol Metab 2020;105:dgz177. [PMID: 31689348 DOI: 10.1210/clinem/dgz177] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
15 Finken MJJ, van der Steen M, Smeets CCJ, Walenkamp MJE, de Bruin C, Hokken-Koelega ACS, Wit JM. Children Born Small for Gestational Age: Differential Diagnosis, Molecular Genetic Evaluation, and Implications. Endocr Rev 2018;39:851-94. [PMID: 29982551 DOI: 10.1210/er.2018-00083] [Cited by in Crossref: 35] [Cited by in F6Publishing: 35] [Article Influence: 11.7] [Reference Citation Analysis]
16 He D, Li Y, Yang W, Chen S, Sun H, Li P, Zhang M, Ban B. Molecular diagnosis for growth hormone deficiency in Chinese children and adolescents and evaluation of impact of rare genetic variants on treatment efficacy of growth hormone. Clin Chim Acta 2022;524:1-10. [PMID: 34826401 DOI: 10.1016/j.cca.2021.11.021] [Reference Citation Analysis]